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线性分子式:
C6H4-1,3-(CHO)2
化学文摘社编号:
分子量:
134.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-935-8
Beilstein/REAXYS Number:
1561038
MDL number:
Assay:
97%
InChI key
IZALUMVGBVKPJD-UHFFFAOYSA-N
InChI
1S/C8H6O2/c9-5-7-2-1-3-8(4-7)6-10/h1-6H
SMILES string
O=Cc1cccc(C=O)c1
assay
97%
mp
87-88 °C (lit.)
functional group
aldehyde
Quality Level
General description
间苯二甲醛参与碱催化的 Knoevenagel 缩合反应。
Application
间苯二甲醛用于双核钉联吡啶络合物的合成。
Packaging
玻璃瓶封装
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
The effect of outer-sphere acidity on chemical reactivity in a synthetic heterogeneous base catalyst.
John D Bass et al.
Angewandte Chemie (International ed. in English), 42(42), 5219-5222 (2003-11-06)
Johanna Andersson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(36), 11037-11046 (2010-08-04)
The binuclear ruthenium complex [μ-bidppz(phen)(4)Ru(2)](4+) has been extensively studied since the discovery of its unusual threading intercalation interaction with DNA, a binding mode with extremely slow binding and dissociation kinetics. The complex has been shown to be selective towards long
商品
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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